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Hydrochloric Acid → 1-Cyano-1-(2-methoxy-3,5-dibromophenyl)cyclohexane

HRID 444102
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반응식

HRID 444102 반응식
[H-].[Na+].Br[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]Br.[Br:10][C:11]1[CH:16]=[C:15]([Br:17])[CH:14]=[C:13]([CH2:18][C:19]#[N:20])[C:12]=1[O:21][CH3:22].Cl>CN(C)C=O.O>[C:19]([C:18]1([C:13]2[CH:14]=[C:15]([Br:17])[CH:16]=[C:11]([Br:10])[C:12]=2[O:21][CH3:22])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1)#[N:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 81001,5-DibromopentaneHCID 24758Sodium hydrideHCID 205361852,4-Dibromo-6-cyanomethylanisole

생성물 1

HCID 205362401-Cyano-1-(2-methoxy-3,5-dibromophenyl)cyclohexane

시약·촉매·용매 2

HCID 962Water용매
HCID 6228
Dimethylformamide
용매
2회

실험 절차

To a stirred suspension of sodium hydride (7 g) in dry dimethylformamide (200 ml) was added a solution of 1,5-dibromopentane (20 ml) and the product of stage (d) in dimethylformamide (40 ml), keeping the temperature at 20°-30° C. The mixture was stirred for 30 minutes, water was added cautiously, and was then poured into ice water. Hydrochloric acid was added and the mixture was extracted with dichloromethane, washed with water and brine, dried over magnesium sulphate and filtered, and the solvent was removed to give a pale brown oil which slowly crystallised. Recrystallisation from ethanol gave the title product as yellow crystalls, mp 100°-102° C.

후처리

  1. customat 20°-30° C
  2. extractionthe mixture was extracted with dichloromethane
  3. washwashed with water and brine
  4. dry with materialdried over magnesium sulphate
  5. filtrationfiltered
  6. customthe solvent was removed
  7. customto give a pale brown oil which
  8. customslowly crystallised
  9. customRecrystallisation from ethanol

출처 및 근거

ORD 기록
ord-85f5274eb87044a296136b774044700d
출처 데이터셋
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04263037

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